Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,440 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,440 in last 12 months

Showing 2386123880 of 50,117 recalls

Medical DeviceOctober 17, 2018· Richard Wolf GmbH

Recalled Item: Richard Wolf Bronchoscope Tubes Recalled by Richard Wolf GmbH Due to There...

The Issue: There is a potential deficiency of the TEXAS Bronchoscope Tube product. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-402 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-400 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-RFP-456 Recalled by NxStage Medical, Inc....

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-401 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-RFP-454 Recalled by NxStage Medical, Inc....

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-404 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-406 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-403 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 16, 2018· Bakkavor Foods USA, Inc.

Recalled Item: Trader Joe's Tomato & Basil Hummus Dip Recalled by Bakkavor Foods USA, Inc....

The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2018· Bakkavor Foods USA, Inc.

Recalled Item: Trader Joe's Hummus quartet Recalled by Bakkavor Foods USA, Inc. Due to...

The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2018· Carl Zeiss Meditec, Inc.

Recalled Item: The PLEX Elite 9000 Recalled by Carl Zeiss Meditec, Inc. Due to Under...

The Issue: Under certain fault conditions, the existing design may expose the operator...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Septishield II Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing